Validation of a Pediatric-Specific Abstinence Syndrome Assessment Tool

Withdrawn

• Conditions: Substance Withdrawal Syndrome

• Registration Number: NCT00792415
• Lead Sponsor: Banner Health

Brief Summary

The purpose of this study is to assess the validity and reliability of an abstinence syndrome assessment tool used in pediatric patients with iatrogenic opioid dependence.

Detailed Description

None available.

Study Timeline

• Study First Submitted: 2008-11-17
• Study First Submitted QC: 2008-11-17
• Study First Posted: 2008-11-18
• Study Start: 2009-11
• Primary Completion: 2010-04
• Study Completion: 2010-12
• Status Verified: 2025-02
• Last Update Submitted: 2025-02-07
• Last Update Posted: 2025-02-11

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: 75

Inclusion Criteria

• Pediatric Intensive Care Unit patients ages 2 weeks to 18 years
• Patients receiving continuous opioid infusions for 5 days (at least 120 hours) or more

Exclusion Criteria

• Attending discretion
• Patients with deterioration of medical status requiring interventions of pain control, surgery, sedation, or re-intubation

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Total scores of abstinence syndrome symptoms	Up to 23 days	None available - PI no longer with Banner

Secondary Outcome Measures

Name	Time	Method
Expert opinion on abstinence syndrome	Up to 23 days	None available - PI no longer with Banner

Trial Locations

Locations (1)

Cardon Children's Medical Center; 🇺🇸 Mesa, Arizona, United States